937118
QPhos Pd G3 ChemBeads
Synonym(s):
QPhos G3 Palladacycle ChemBeads, QPhos Palladacycle ChemBeads, [2′-(Amino-κN)[1,1′-biphenyl]-2-yl-κC][1′-[bis(1,1-dimethylethyl)phosphino]-1,2,3,4,5-pentaphenylferrocene](methanesulfonato-κO)palladium ChemBeads
About This Item
form
solid
Quality Level
composition
, 4-6 wt. % (loading)
reaction suitability
reagent type: catalyst
SMILES string
O=S(=O)([O-][Pd+2]1([C-]=2C=CC=CC2C=3C=CC=CC3[NH2]1)[P](C(C)(C)C)(C(C)(C)C)[C-]45[CH]6=[CH]7[CH]8=[CH]4[Fe+2]7869%10%11%125C=%13(C=%14C=CC=CC%14)C%12(C=%15C=CC=CC%15)=C%11(C=%16C=CC=CC%16)[C-]%10(C=%17C=CC=CC%17)C%139C=%18C=CC=CC%18)C
InChI
InChI=1S/C35H25.C13H22P.C12H10N.CH4O3S.Fe.Pd/c1-6-16-26(17-7-1)31-32(27-18-8-2-9-19-27)34(29-22-12-4-13-23-29)35(30-24-14-5-15-25-30)33(31)28-20-10-3-11-21-28;1-12(2,3)14(13(4,5)6)11-9-7-8-10-11;13-12-9-5-4-8-11(12)10-6-2-1-3-7-10;1-5(2,3)4;;/h1-25H;7-10H,1-6H3;1-6,8-9H,13H2;1H3,(H,2,3,4);;/q3*-1;;2*+2/p-1
InChI key
NNVAEYGNFLUPRU-UHFFFAOYSA-M
General description
- The synthesis of complex druglike moleucle via Negisihi couplings using a high-throughput experimentation approach.[1]
- The regioselective arylboration of isoprene using cooperative Pd/Cu catalysis.[2]
- The total synthesis of Phainanoid A and its synthetic analogues.[3][4]
Application
For general uses, product is also available in powdered form 903027
Features and Benefits
related product
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
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